Issue 67, 2016, Issue in Progress

Synthesis of β-phthalimido-alcohols via regioselective ring opening of epoxide by using reusable basic magnetic nano particles and their biological investigation

Abstract

In this work, tetra butyl ammonium hydroxide ([Bu4N]OH) and magnetic nano particles (Fe3O4@SiO2@(CH2)3NH2) were introduced as efficient catalysts for the regioselective ring opening of epoxides including aromatic and aliphatic of epoxides to give the corresponding β-phthalimido-alcohols under mild conditions. A various range of β-phthalimido-alcohols as new compounds were prepared and fully characterized by IR, 1H as well as 13C NMR and mass spectra. Also the synthesized compounds were studied for antioxidant properties by DPPH free radical scavenging assay. The results indicated that studied β-phthalimido-alcohols derivatives have effective antioxidant functions (IC50: 0.142–0.356 mg mL−1) in compare with BHT (IC50: 0.122 mg mL−1) and ascorbic acid (IC50: 0.146 mg mL−1) as standards. This may be a new health-care food and drug supplement for special use in the future.

Graphical abstract: Synthesis of β-phthalimido-alcohols via regioselective ring opening of epoxide by using reusable basic magnetic nano particles and their biological investigation

Supplementary files

Article information

Article type
Paper
Submitted
23 Mar 2016
Accepted
17 Jun 2016
First published
17 Jun 2016

RSC Adv., 2016,6, 62460-62466

Synthesis of β-phthalimido-alcohols via regioselective ring opening of epoxide by using reusable basic magnetic nano particles and their biological investigation

M. A. Zolfigol, A. R. Moosavi-Zare, M. Zarei, A. Zare, E. Noroozizadeh, R. Karamian and M. Asadbegy, RSC Adv., 2016, 6, 62460 DOI: 10.1039/C6RA07660B

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